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Publication : Childhood absence epilepsy: genes, channels, neurons and networks.

First Author  Crunelli V Year  2002
Journal  Nat Rev Neurosci Volume  3
Issue  5 Pages  371-82
PubMed ID  11988776 Mgi Jnum  J:76681
Mgi Id  MGI:2179932 Doi  10.1038/nrn811
Citation  Crunelli V, et al. (2002) Childhood absence epilepsy: genes, channels, neurons and networks. Nat Rev Neurosci 3(5):371-82
abstractText  Childhood absence epilepsy is an idiopathic, generalized non-convulsive epilepsy with a multifactorial genetic aetiology. Molecular-genetic analyses of affected human families and experimental models, together with neurobiological investigations, have led to important breakthroughs in the identification of candidate genes and loci, and potential pathophysiological mechanisms for this type of epilepsy. Here, we review these results, and compare the human and experimental phenotypes that have been investigated. Continuing efforts and comparisons of this type will help us to elucidate the multigenetic traits and pathophysiology of this form of generalized epilepsy.
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